Lot numbers can be found on the outside label of a product:
Please log in for operation!
*For research and further manufacturing use only, not for direct human use.
Structure of 932374-77-1
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
1-Bromo-5-fluoro-4-nitro-2-(trifluoromethyl)benzene features a highly electron-deficient aromatic core stabilized by strong inductive effects from the trifluoromethyl and nitro groups. This configuration enables efficient palladium-catalyzed cross-coupling reactions under mild conditions, with the bromo group serving as a reliable handle for C–C bond formation. The molecule exhibits excellent bench stability and compatibility with diverse reaction environments.
1-Bromo-5-fluoro-4-nitro-2-(trifluoromethyl)benzene serves as a versatile building block for constructing complex fluorinated aromatic scaffolds. Its orthogonal reactivity enables palladium-catalyzed cross-coupling, nucleophilic substitution, and sequential functionalization. The trifluoromethyl and nitro groups enhance metabolic stability and modulate electronic properties, while the bromo and fluoro substituents provide distinct sites for further derivatization. Bench-stable and compatible with standard purification protocols, it facilitates efficient synthesis of advanced intermediates for pharmaceutical and agrochemical applications.
|
GHS Pictogram :
|
GHS No : GHS07
|
|
Signal Word : Warning
|
UN#: N/A
|
|
Class : N/A
|
Packing Group : N/A
|
|
Hazard Statements : H302-H315-H319-H335
|
|
|
Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P362+P364-P405-P501
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: